Variant DetailsVariant: dgv444e199Internal ID | 20123746 | Landmark | | Location Information | | Cytoband | 15q11.2 | Allele length | Assembly | Allele length | hg38 | 10351 | hg19 | 10351 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | esv2660573, esv2676084 | Samples | NA19005, NA18973, NA19000, NA19072, NA19083 | Known Genes | SNRPN | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | dgv444e199
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
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