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Fig. 2 | Genome Medicine

Fig. 2

From: X-CNV: genome-wide prediction of the pathogenicity of copy number variations

Fig. 2

Strategy 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 subpopulations

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