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Table 2 Indications for testing

From: Laboratory performance of genome-wide cfDNA for copy number variants as compared to prenatal microarray

Screening indication

N (Percent)

Percent

Maternal age > 35

142

20.3

Positive serum screening

131

18.7

Ultrasound finding(s)

208

29.7

Personal/family history of CNV or aneuploidy

12

1.7

Other

19

2.7

Multiple indications

189

27.0

Total samples

701