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. Author manuscript; available in PMC: 2020 Jul 23.
Published in final edited form as: Prog Mol Biol Transl Sci. 2016 Mar 23;140:1–45. doi: 10.1016/bs.pmbts.2015.12.003

Figure 4.

Figure 4

Figure 4

(A) Chromosome microarray results for PWS deletion subtypes. High resolution chromosome microarray using CNV and SNP probes to identify typical 15q11-q13 deletions in PWS classified as Type I involving breakpoints BP1 and BP3 and Type II involving breakpoints BP2 and BP3. (B) Chromosome Microarray Results for Uniparental Maternal Disomy 15. High resolution chromosome microarray using CNV and SNP probes to identify the maternal disomy 15 subtype (segmental isodisomy 15, isodisomy 15, and heterodisomy 15).