An Atypical 15q11.2 Microdeletion Not Involving SNORD116 Resulting in Prader–Willi Syndrome

Table 2

Single nucleotide polymorphism (SNP) analysis data.

SNPs	Patient	Father	Mother
Chr15 : 24,830,384 (build hg38)	GA	GA	GA
rs61994705	GG	GC	GC
rs187852468	GG	GC	GC
rs11161153	GG	GG	GC
rs71461569	CC	AC	AC
rs61999138	TC	CC	TC

SNPs interrogated in both the patient and her parents to further narrow the smallest possible deleted region in the patient presented.