Fig. 2From: 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 percentages of CNVs distinct for type of aberrations; (b) percentages of CNVs distinct for hereditary pattern [NA: not available]Back to article page