Copy number variation (CNV) identified by array CGH in the patient.
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Shown are the CNV coordinates in hg18 (Build 36.3) for the gains and losses of DNA sequences on the listed chromosomes (Chr.) The number of individuals or occurrence in the Watson genome are indicated in the frequency data, which are derived from the Toronto Database of Genomic Variants (DGV).
创建时间：
2012-12-27
