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%) |