Variant DetailsVariant: dgv1218e199Internal ID | 20124520 | Landmark | | Location Information | | Cytoband | 7q11.23 | Allele length | Assembly | Allele length | hg38 | 585559 | hg19 | 585559 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | esv2667579, esv2658510, esv2675417, esv2673053 | Samples | HG00542, NA12058, HG00689, HG00346, HG00690, HG00404, NA19469, NA19248 | Known Genes | DTX2, DTX2P1-UPK3BP1-PMS2P11, FDPSP2, LOC100132832, LOC100133091, POMZP3, UPK3B | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | dgv1218e199
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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