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Table 5 Pregnancy outcomes of 958 participants with follow-up data

From: Comprehensive chromosomal abnormality detection: integrating CNV-Seq with traditional karyotyping in prenatal diagnostics

 

Live birth (N = 854)

Termination (N = 104)

Total (N = 958)

Chromosomal aneuploidy

4 (11.4%)

31 (88.6%)

35 (100.0%)

 T21

1 (5.0%)

19 (95.0%)

20 (100.0%)

 T18

0 (0.0%)

4 (100.0%)

4 (100.0%)

 T13

0 (0.0%)

2 (100.0%)

2 (100.0%)

 Sex chromosome abnormality

3 (33.3%)

6 (66.7%)

9 (100.0%)

P/LP CNVs

21 (39.6%)

32 (60.4%)

53 (100.0%)

 Microdeletion

13 (34.2%)

25 (65.8%)

38 (100.0%)

 microduplication

8 (53.3%)

7 (46.7%)

15 (100.0%)

VUS

829 (95.3%)

41 (4.7%)

870 (100.0%)

  1. VUS: variants of uncertain significance