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