Variant DetailsVariant: esv3587421Internal ID | 6627725 | Landmark | | Location Information | | Cytoband | 1q21.1 | Allele length | Assembly | Allele length | hg38 | 101907 | hg19 | 101886 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv10113678, essv10113677, essv10113676, essv10113675 | Samples | NA19066, HG01537, HG00844, HG00698 | Known Genes | CD160, GPR89A, LOC100288142, NBPF10, PDZK1, RNF115 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3587421
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
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