public PathologyReportContainer GetReport()
        {
            var RequestedDate            = new DateTimeOffset(2020, 09, 19, 00, 00, 00, TimeSpan.FromHours(10));
            var CollectionDateTime       = new DateTimeOffset(2020, 09, 20, 08, 20, 00, TimeSpan.FromHours(10));
            var SpecimenReceivedDateTime = new DateTimeOffset(2020, 09, 20, 09, 35, 00, TimeSpan.FromHours(10));
            var ReportReleaseDateTime    = new DateTimeOffset(2020, 09, 22, 11, 15, 00, TimeSpan.FromHours(10));
            var ObservationDateTime      = ReportReleaseDateTime.Subtract(TimeSpan.FromMinutes(5));

            return(new PathologyReportContainer()
            {
                PathologyReport = new PathologyReport()
                {
                    PerformingLaboratory = LaboratoryFactory.GetPITUSLaboratory(),
                    Patient = PatientFactory.GetNormanMANNING(),
                    Request = new Request()
                    {
                        RequestedDate = RequestedDate,
                        OrderNumber = "00000005",
                        RequestingFacility = new Organisation()
                        {
                            Name = "Sunrise Hospital Metabolic Clinic",
                            Identifier = new Identifier()
                            {
                                Value = "75C38DF6-BE0B-4287-8D46-6395CACAAD7A",
                                Type = IdentifierType.GUID
                            }
                        },
                        RequestingApplication = "Best Practice 1.8.5.743",
                        RequestingProvider = ProviderFactory.GetTrishFamilyDr(MedicareProviderNumber: "2359622W"),
                        ClinicalNotes = "? Hereditary haemochromatosis. Arthritis, increased iron stores",
                        CallBackPhoneNumber = null,
                        CopyToList = new List <Provider>()
                        {
                            ProviderFactory.GetGeneticsClinic(),
                            ProviderFactory.GetBjornGeneticCounsellor()
                        }
                    },
                    PdfFileName = "Exemplar Report Haemochromatosis gene screening v1.5.pdf",
                    ReportList = new List <Report>()
                    {
                        new Report()
                        {
                            ReportId = "1978881777",
                            CollectionDateTime = CollectionDateTime,
                            SpecimenReceivedDateTime = SpecimenReceivedDateTime,
                            ReportReleaseDateTime = ReportReleaseDateTime,
                            ReportType = new ReportType()
                            {
                                Local = new Code()
                                {
                                    Term = "HFE", Description = "Haemochromatosis gene screening"
                                },
                                Snomed = new Code()
                                {
                                    Term = "401085002", Description = "Haemochromatosis gene screening test"
                                }
                            },
                            ReportStatus = ResultStatusType.Final,
                            Department = DiagnosticService.Genetics,
                            ReportingPathologist = ProviderFactory.GetKondoPathologist(),
                            Panel = new Panel()
                            {
                                ResultList = new List <Result>()
                                {
                                    new Result()
                                    {
                                        Type = new ResultType()
                                        {
                                            Local = new Code()
                                            {
                                                Term = "C28Y",
                                                Description = "C28Y mutation analysis"
                                            },
                                            Lonic = null,
                                        },
                                        DataType = "ST",
                                        Value = "Not Detected",
                                        Units = null,
                                        ReferenceRange = null,
                                        AbnormalFlag = "N",
                                        ObservationDateTime = ObservationDateTime,
                                        Status = ResultStatusType.Final,
                                        ChildResultList = null
                                    },
                                    new Result()
                                    {
                                        Type = new ResultType()
                                        {
                                            Local = new Code()
                                            {
                                                Term = "H63D",
                                                Description = "H63D mutation analysis"
                                            },
                                            Lonic = null,
                                        },
                                        DataType = "ST",
                                        Value = "Homozygous",
                                        Units = null,
                                        ReferenceRange = null,
                                        AbnormalFlag = "N",
                                        ObservationDateTime = ObservationDateTime,
                                        Status = ResultStatusType.Final,
                                        ChildResultList = null
                                    },
                                    new Result()
                                    {
                                        Type = new ResultType()
                                        {
                                            Local = new Code()
                                            {
                                                Term = "RES",
                                                Description = "Results"
                                            },
                                            Lonic = null,
                                        },
                                        DataType = "FT",
                                        Value = "Two copies of the p.His63Asp variant were detected in the patient. The p.Cys282Tyr variant was not detected.\\.br\\" +
                                                "The diagnosis of the most common form of HFE-related hereditary haemochromatosis is excluded.\\.br\\",
                                        Units = null,
                                        ReferenceRange = null,
                                        AbnormalFlag = "N",
                                        ObservationDateTime = ObservationDateTime,
                                        Status = ResultStatusType.Final,
                                        ChildResultList = null
                                    },
                                    new Result()
                                    {
                                        Type = new ResultType()
                                        {
                                            Local = new Code()
                                            {
                                                Term = "INTER",
                                                Description = "Interpretation"
                                            },
                                            Lonic = null,
                                        },
                                        DataType = "FT",
                                        Value = "Hereditary haemochromatosis (HH) is a recessive genetic disorder of iron metabolism. Greater than 90% of HFE\\.br\\" +
                                                "related hereditary haemochromatosis is associated with homozygosity for p.(Cys282Tyr) (c.845G>A; aka p.C282Y).\\.br\\" +
                                                "Compound heterozygosity for p. (Cys282Tyr) and p. (His63Asp) (c.187C>G; aka p.H63D) may be a risk factor\\.br\\" +
                                                "predisposing to mild to moderate forms of iron overload when in association with other risk factors. Both mutations\\.br\\" +
                                                "are detected by real-time PCR amplification and fluorescent detection of alleles.",
                                        Units = null,
                                        ReferenceRange = null,
                                        AbnormalFlag = "N",
                                        ObservationDateTime = ObservationDateTime,
                                        Status = ResultStatusType.Final,
                                        ChildResultList = null
                                    }
                                }
                            }
                        }
                    }
                }
            });
        }