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Table 2 Independent predictors of pathogenic CNV

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

  1. SE standard error, OR odds ratio, CI confidence interval, VSD ventricular septal defect