Variant DetailsVariant: esv2673844Internal ID | 9593263 | Landmark | | Location Information | | Cytoband | 10q26.3 | Allele length | Assembly | Allele length | hg38 | 119 | hg19 | 119 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6566310, essv5757191, essv6280480, essv5964007, essv5992003, essv6086656, essv5987075, essv6531649, essv6050454, essv6286931, essv5972711, essv6124224, essv6421264, essv5839126, essv6445041, essv6320042, essv5815523, essv5546818, essv5946969, essv6368977 | Samples | HG01374, NA20796, HG01366, HG00281, HG00137, HG01183, HG01136, HG01073, HG01497, HG01334, NA12144, HG00246, HG01107, HG00254, HG00375, HG01357, HG00237, HG00111, NA20528, HG01125 | Known Genes | MGMT | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2673844
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 20 | Observed Complex | 0 | Frequency | n/a |
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