Variant DetailsVariant: esv3638893 Internal ID | 6678990 | Landmark | | Location Information | | Cytoband | 16q22.1 | Allele length | Assembly | Allele length | hg38 | 2780 | hg19 | 2780 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15501530, essv15501567, essv15501561, essv15501574, essv15501528, essv15501572, essv15501564, essv15501558, essv15501526, essv15501542, essv15501537, essv15501568, essv15501571, essv15501533, essv15501532, essv15501548, essv15501535, essv15501531, essv15501576, essv15501560, essv15501550, essv15501551, essv15501534, essv15501554, essv15501544, essv15501527, essv15501577, essv15501545, essv15501569, essv15501540, essv15501563, essv15501552, essv15501549, essv15501541, essv15501565, essv15501539, essv15501570, essv15501555, essv15501538, essv15501547, essv15501575, essv15501543, essv15501536, essv15501579, essv15501553, essv15501566, essv15501573, essv15501556, essv15501557, essv15501546, essv15501578, essv15501562, essv15501559, essv15501529 | Samples | NA19701, HG03484, NA18861, HG01885, HG03126, HG03518, NA19098, HG03372, NA19107, HG03572, HG03082, NA19379, HG03168, HG02485, HG03212, NA19235, HG03380, HG03583, HG02477, HG02009, HG03054, HG03132, NA19984, HG01162, HG02511, HG02554, HG03457, HG03428, NA18910, HG01880, HG03124, HG03311, NA18856, HG02666, HG02256, HG02332, HG02586, NA19321, HG01894, NA19037, NA20351, HG03304, HG03432, HG01912, NA19468, HG03279, NA19185, HG02768, HG03401, NA19030, NA18505, NA19129, NA18511, HG03166 | Known Genes | RANBP10 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3638893
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 54 | Observed Complex | 0 | Frequency | n/a |
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