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
b(SE)
OR
95%CI
p value
Prematurity
2.58 (0.89)
13.7
2.28–76.09
0.004
VSD
1.52 (0.75)
5.78
1.06–19.86
0.042
Dysmorphisms
1.41 (0.44)
4.09
1.73–9.66
0.001