Figure 4
From: Incidental copy-number variants identified by routine genome testing in a clinical population
An analysis of multigene copy-number variants (CNVs) reveals additional incidental variants. CNVs affecting disease genes for dominant Mendelian cancer-predisposition syndromes and spanning up to 20 genes per CNV were identified. As CNVs extending beyond a single gene are examined, additional incidental variants are revealed. Genes listed under each “step” of the graph are those rearranged by CNVs affecting the number of genes indicated on the x-axis. The number of subjects with such a CNV, if greater than one, is shown in parentheses. Nineteen additional CNVs, affecting 13 unique genes, identified as CNVs spanning from 2 to 20 genes are considered.
