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. 2022 Apr 27;13:81. doi: 10.4103/ijpvm.IJPVM_572_20

Table 1.

Evaluation and compare the incidence of chromosomal abnormalities based on final risk and NT percentile

Group characteristics NT ≥99% (117) P: 0.002 NT <99% (17) 1/10≤ risk P: 0.003 NT<99% (119) 1/50≤ risk <1/10 P: 0.03 NT <99% (119) 1/100≤ risk <1/50 P: 0.36 NT <99% (254) 1/250≤ risk <1/100 P: 0.16 NT <99% (131) 1/250> risk P: 0.1
Normal 104 (88.88%) 12 (76.5%) 103 (84.9%) 115 (95.8%) 241 (93.8%) 136 (93.9%)
Numeric 12 (10.3%) 4 (23.5%) 9 (7.6%) 2 (1.7%) 4 (1.7%) 1 (0.8%)
Down syndrome 12 3 8 2 2 0
Others 0 1 1 0 2 1
De novo structural 1 (0.9%) 1 (5.9%) 6 (5%) 2 (1.7%) 7 (2.9%) 6 (46%)
Numeric cumulative 12 (37.5%) 16 (50%) 25 (78.125%) 27 (84.375%) 31 (96.875%) 32 (100%)
Structural cumulative 1 (43.47%) 2 (8.695%) 8 (34.782%) 10 (43.478%) 17 (73.913%) 23 (100%)
Total cumulative 13 (23.63%) 18 (32.72%) 33 (60%) 37 (67.27%) 48 (87.27%) 55 (100%)