Fig. 1From: Characterization of a de novo sSMC 17 detected in a girl with developmental delay and dysmorphic featuresThe result of aCGH indicating microduplication of chromosome 17 (arr[hg19]17q11.1q11.2(25,403,446-27,716,930)x3). Whole chromosome 17 and a close-up of duplicated region with annotated genes is visualizedBack to article page