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Fig. 3 | Italian Journal of Pediatrics

Fig. 3

From: 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 anomalies

Fig. 3

a 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 chromosomes

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