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Table 3 Frequencies of NCA, P/LP CNV and ROH between singleton and twin fetuses with CHDs

From: Contribution of genetic variants to congenital heart defects in both singleton and twin fetuses: a Chinese cohort study

CMA results

Total    (n = 1118)

Isolated    (n = 887)

Nonisolated    (n = 231)

p

Singleton fetuses with CHD

Twin fetuses with CHD

p (Singleton vs. Twin)

Total    (n = 961)

Isolated  (n = 778)

Nonisolated  (n = 183)

P

Total  (n = 157)

Isolated  (n = 109)

Nonisolated (n = 48)

p

CA

NCA (n, %)

102 (9.1)

39 (4.4)

63 (27.3)

 < 0.001*

80 (8.3)

32 (4.1)

48 (26.2)

 < 0.001*

22 (14.0)

7 (6.4)

15 (31.3)

 < 0.001*

0.022*

CNV (n, %)

95 (8.5)

68 (7.7)

27 (11.7)

0.051*

83 (8.6)

60 (7.7)

23 (12.6)

0.035*

12 (7.6)

8 (7.3)

4 (8.3)

0.829#

0.679*

Total (n, %)

197 (17.6)

107 (12.1)

90 (39.0)

 < 0.001*

163 (17.0)

92 (11.8)

71 (38.8)

 < 0.001*

34 (21.7)

15 (13.8)

19 (39.6)

 < 0.001*

0.152*

ROH (n, %)

4 (0.4)

2 (0.2)

2 (0.9)

0.191#

4 (0.4)

2 (0.3)

2 (1.1)

0.166#

0

0

0

–

–

 
  1. CA Chromosomal abnormalities; CHD Congenital heart defect; CMA Chromosomal microarray analysis; CNV Copy number variant; NCA Numerical chromosomal abnormality; ROH Region of homozygosity
  2. *Chi-square test; #Fisher's exact test