Table 2. Inherited CNVs identified in patients with ASD classified as pathogenic, likely pathogenic or of unknown significance.

ID	Cytoband	Type	Location	Size (kb)	Genes	Classification	Inheritance
SES3	10q11.22	Gain	46776777-47939116	1162	GPRIN2, FAM35B2, ANTXRL, FAM35B, SYT15, AGAP9, ANXA8L2, PPYR1, FAM21B, FAM25C, LOC642826, ANXA8, LOC643650	Unknown significance	Mother
LAS9	10q11.22	Gain	46950168-47939116	989	FAM21B/25B/35B2, SYT15, ANXA8L2, ANTXRL, PPYR1, AGAP9, LOC643650/642826, GPRIN2, FAM25G	Unknown significance	Father
	7q22.3	Gain	105890353-106064794	174	NAMPT	Unknown significance	Father & Mother
LAS17	2p16.3	Loss	51166006-51302668	137	NRXN1	Pathogenic	Father
CLIN22	14q12	Gain	31642542-31778371	136	HECTD1, HEATR5A	Unknown significance	Mother
CLIN24	20p11.23	Loss	20441027-20573017	132	RALGAPA2	Unknown significance	Mother
BAK41	Yp11.31	Gain	2867178-3222952	356	LINC00278	Unknown significance	Father
	Yp11.2	Gain	3973124-4271373	298	No genes	Unknown significance	Father
BAK42	4q28.3	Loss	138092729-138196101	103	No genes	Unknown significance	Mother
	5q35.2	Loss	175438045-175638617	201	FAM153B, LOC100507387, LOC643201	Unknown significance	Father
	8q22.1	Gain	97151500-97303937	152	GDF6, MTERFD1, PTDSS1, UQCRB	Unknown significance	Mother
BAK45	1q43	Gain	237517711-238090569	573	RYR2, LOC100130331, ZP4	Likely pathogenic	Mother
	Xp22.33	Gain	1841391-2303322	462	DHRSX	Unknown significance	Father