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Table 2 The coincidence rate of each abnormal chromosome detected by NIPT

From: Performance of non-invasive prenatal testing for foetal chromosomal abnormalities in 1048 twin pregnancies

Abnormal chromosome

NIPT high-risk

Coincidence rate of prenatal diagnosis

T21

2

1/2

T18

1

0/1

T13

45,X

5

0/5

47,XXX

1

0/1

47,XXY

1

0/1

Microdeletion

1

1/1

Microduplication

2

0/2

Total

13

2/13