Table 3; online only:

Summary of copy number variation for subjects with HLHS hosting abnormal/pathogenic CNVs

CMA Pathologic Variants
Subject	CNV		Clinical Presentation or Syndrome
1	Xp22.33q28	Loss	Turner syndrome, renal pyelectasis, cystic kidneys  bilaterally
2	1p36.33p36.32	Gain	Gastroparesis and esophageal dysmotility
3	Xp22.33q28	Loss	Turner syndrome
4	15q11.2,	Loss	Turner Syndrome
	Xp22.33q28,	Loss
	Yp11.31q11.1	Gain
5	X,	Loss	Turner Syndrome
	Yp11.31p11.2	Gain
6	12p13.33p11.1	Gain	Pallister-Killian syndrome
7	18q23	Gain	Partial Trisomy 18q and dysmorphic features
8	13q13.1	Gain	BRCA2 Duplication
9	22q11.21	Loss	Cleft lip/palate (features of DiGeorge Syndrome)