Variant DetailsVariant: esv2677132 Internal ID | 9596551 | Landmark | | Location Information | | Cytoband | 11q25 | Allele length | Assembly | Allele length | hg38 | 945 | hg19 | 945 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6445228, essv5958758, essv6527802, essv6252446, essv5475315, essv6298357, essv6066448, essv6150827, essv6463773, essv6463044, essv6027957, essv6311939, essv6416106, essv6228313, essv6267616, essv6437592, essv6254118, essv5465032, essv5953196, essv5732311, essv5557535, essv6360053, essv5963275, essv6174281, essv6569619, essv6194753, essv5904882, essv5568656, essv6306693 | Samples | NA19909, NA19204, NA19377, HG01366, NA19382, NA18498, NA19904, NA19384, NA20291, NA19385, NA19172, NA19471, NA19901, NA19247, NA19455, NA19236, NA18871, NA18856, NA19099, NA19395, NA19108, NA18517, NA19435, NA20804, NA19713, NA19093, NA19213, NA19312, NA18487 | Known Genes | NTM | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | High quality site | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2677132
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 29 | Observed Complex | 0 | Frequency | n/a |
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