Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants

Table 1 Demographic and deletion information for 16p11.2del training signature cases and age-, sex-matched controls

Sample ID	Sex	Age (years)	ASD status	16p11.2del (600 kb region) coordinates	Deletion size (kb)	Inheritance
435	M	12	Unknown	29,656,657–30,190,593	534	Unknown
516	M	7	Unknown	29,656,657–30,190,593	534	Unknown
639	F	13	Unknown	29,592,751–30,190,593	598	Unknown
797	M	7	Unknown	29,590,493–30,190,593	600	Unknown
871	M	10	Unknown	29,590,493–30,190,593	600	Unknown
293	M	5	Unknown	29,567,295–30,178,406	611	Unknown
3-0269-000	M	4	ASD	29,567,309–30,177,807	610	Maternal
1-0019-004	M	7.5	ASD	29,652,799–30,199,507	547	De novo
7-0229-003	M	11.5	ASD	29,567,295–30,177,916	611	Unknown
EP15W	M	13	Control
EP16W	F	2	Control
EP17W	F	4	Control
EP1W	F	8	Control
EP22W	M	4	Control
EP2W	F	10	Control
EP3W	F	13	Control
EP4W	M	13	Control
EP5W	F	8	Control
EP6W	M	13	Control
EP7W	M	9	Control
EP8W	M	8	Control
EP9W	M	11	Control
EP51	M	12	Control
EP60W	M	12	Control
460/2048	M	11.5	Control
EP32W	M	6	Control
EP45W	M	10	Control
EP59W	M	6	Control
EP57W	M	7	Control
CT0011-003	M	4	Control
MK-311/1601	M	10	Control
KA-352/1734	M	7	Control

ISSN: 1868-7083