RuleSet: CopyNumberVariant * CopyNumberVariant 0..* BackboneElement "Einfache Variante" * Chromosom 1..1 code "Chromosom" * StartPositionsbereich 1..1 integer "Start-Positionsbereich" * EndePositionsbereich 1..1 integer "Ende-Positionsbereich" * TotalCN 1..1 integer "Total CN" * RelativeCN 1..1 string "Relative CN" * CNA 1..1 integer "CNA" * CNB 1..1 integer "CNB" * ReportedAffectedGenes 1..1 string "Reported Affected Genes" * ReportedFocality 1..1 string "Reported Focality" * Type 1..1 string "Type" * CopyNumberNeutralLoH 1..1 string "Copy-Number-Neutral LoH" RuleSet: CopyNumberVariantMapping * CopyNumberVariant -> "MII_PR_MolGen_Variante" * Chromosom -> "MII_PR_MolGen_Variante.component[chromosome-identifier]" * StartPositionsbereich -> "MII_PR_MolGen_Variante.component[exact-start-end].low" * EndePositionsbereich -> "MII_PR_MolGen_Variante.component[exact-start-end].high" * TotalCN -> "MII_PR_MolGen_Variante.component[copy-number]" * RelativeCN -> "MII_PR_MolGen_Variante.component[relative-copy-number]" * CNA -> "MII_PR_MolGen_Variante.component[cna]" * CNB -> "MII_PR_MolGen_Variante.component[cnb]" * ReportedAffectedGenes -> "MII_PR_MolGen_Variante.component[gene-studied]" * ReportedFocality -> "MII_PR_MolGen_Variante.component[reported-focality]" * Type -> "MII_PR_MolGen_Variante.component[cnv-type]" * CopyNumberNeutralLoH -> "MII_PR_MolGen_Variante.component[copy-number-neutral-loh]"