Variant DetailsVariant: esv3638042Internal ID | 6678140 | Landmark | | Location Information | | Cytoband | 16p13.11 | Allele length | Assembly | Allele length | hg38 | 40654 | hg19 | 40654 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15385676, essv15385654, essv15385657, essv15385656, essv15385671, essv15385660, essv15385670, essv15385674, essv15385663, essv15385673, essv15385668, essv15385665, essv15385661, essv15385662, essv15385664, essv15385652, essv15385681, essv15385655, essv15385680, essv15385667, essv15385653, essv15385678, essv15385651, essv15385650, essv15385669, essv15385658, essv15385682, essv15385675, essv15385677, essv15385672, essv15385666, essv15385659, essv15385679, essv15385649 | Samples | NA18502, HG03548, HG02798, HG03193, HG02952, HG00334, NA20287, NA19404, NA19235, NA19385, NA20342, NA19210, HG02582, HG02678, HG02511, HG01094, NA19461, HG02577, HG03446, HG02884, NA19095, HG01990, HG02455, HG03127, NA19324, NA19467, NA19360, HG02095, HG03097, HG03351, NA19213, HG03072, HG03890, HG03196 | Known Genes | FOPNL | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3638042
| Frequency | Sample Size | 2504 | Observed Gain | 34 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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