. Author manuscript; available in PMC: 2018 Oct 24.

Published in final edited form as: J Hum Genet. 2018 Apr 24;63(7):795–801. doi: 10.1038/s10038-018-0451-x

Table I.

Number of parental CMA cases removed for each genomic disorder

Syndrome	Parental cases removed
SMS	0
WBS	0
PWS/AS	0
VCFS	0
HNPP	1
1q21.1 microdeletion syndrome	1
1q21.1 microduplication	7
15q13.3 microdeletion syndrome	28
16p11.2 microdeletion syndrome	5
16p11.2 microduplication syndrome	12

SMS: Smith-Magenis Syndrome, WBS: Williams-Beuren Syndrome, PWS/AS: Prader-Willi Syndrome/Angelman Syndrome, VCFS: Velocardiofacial Syndrome, HNPP: Hereditary Neuropathy with Liability to Pressure Palsies, CMA: chromosomal microarray