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. 2019 Feb 28;11:36. doi: 10.1186/s13148-019-0633-1

Table 1.

Clinical information, deletion range, and methylation status at SNRPN-DMR in cases enrolled in this study

Cases Phenotype Sex Agea Breakpoint (approximate size) Methylation status at SNRPN-DMRd
Case 1 PWS Male 2 mo Chr15:25,150,978-25,225,535 (75 kb)b Hypermethylated
Case 2 Healthy carrier (father of case 1) Male 36 yr Hypomethylated
Case 3 PWS Female 3 yr Chr15:25,216,569-25,415,670 (200 kb)b Normal
Case 4 AS Female 3 yr Chr15:25,126,774-25,168,037 (41 kb)b Hypomethylated
Case 5 AS Male 4 yr Chr15:25,164,853-25,168,575 (3.7 kb)b Hypomethylated
Case 6 Healthy carrier (mother of case 5) Female 36 yr Normal
PWSLD PWSLD-1 PWS Male 0 mo BP2–3 (5.5 Mb)c Hypermethylated
PWSLD-2 PWS Male 2 mo BP1–3 (6 Mb)c Hypermethylated
PWSLD-3 PWS Male 3 yr BP1–3 (6 Mb)c Hypermethylated
PWSLD-4 PWS Male 8 yr BP1–3 (6 Mb)c Hypermethylated
ASLD ASLD-1 AS Female 9 yr BP2–3 (5.5 Mb)c Hypomethylated
ASLD-2 AS Female 9 yr BP2–3 (5.5 Mb)c Hypomethylated
ASLD-3 AS Male 2 yr BP1–3 (6 Mb)c Hypomethylated
ASLD-4 AS Female 1 yr BP1–3 (6 Mb)c Hypomethylated

PWS Prader-Willi syndrome, AS Angelman syndrome, DMR differentially methylated region, LD large deletion, BP breakpoint

aAge at sample collection (mo months, yr years)

bThe breakpoints were estimated according to the results of aCGH

cThe breakpoints were estimated according to the results of methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA). The locations of BPs are shown in Additional file 2: Figure S1

dMethylation status were examined by MS-MLPA