Fig. 2From: X-CNV: genome-wide prediction of the pathogenicity of copy number variationsStrategy to unify potentially identical CNVs and the general properties of the unified CNVs in a natural population. A Schematic diagram depicting the use of maximal clique algorithm to unify CNVs. B Coverage of unified CNVs on the human genome. C The different lengths between gain and loss, pathogenic and benign, intragenic, and intergenic CNVs. D Proportions of the samples in the subpopulations from DbVar. E Population allele frequency (PAF) of gain and loss in the subpopulationsBack to article page