Fig. 3From: Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomaliesa CNVs distribution on chromosomes; b Correlation of chromosomes’ size (Mb) and number of CNVs for each chromosome; c Correlation of gene density and number of CNVs for each chromosome; d Pathogenic CNVs distribution on chromosomesBack to article page