Figure 3From: Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis Number of total (A), intragenic (B) and extragenic (C) known CNVs reported in the Database of Genomic Variants () per patient http://projects.tcag.ca/variation.Back to article page