Variant DetailsVariant: esv3642262 | Internal ID | 7029032 | | Landmark | | | Location Information | | | Cytoband | 18q12.2 | | Allele length | | Assembly | Allele length | | hg38 | 956 | | hg19 | 956 |
| | Variant Type | CNV loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv15844565, essv15844526, essv15844555, essv15844528, essv15844532, essv15844579, essv15844561, essv15844580, essv15844551, essv15844588, essv15844558, essv15844520, essv15844524, essv15844521, essv15844569, essv15844587, essv15844544, essv15844549, essv15844559, essv15844530, essv15844523, essv15844567, essv15844552, essv15844550, essv15844537, essv15844533, essv15844535, essv15844570, essv15844585, essv15844547, essv15844589, essv15844583, essv15844529, essv15844538, essv15844541, essv15844539, essv15844553, essv15844527, essv15844536, essv15844568, essv15844543, essv15844577, essv15844534, essv15844571, essv15844556, essv15844560, essv15844576, essv15844572, essv15844573, essv15844563, essv15844581, essv15844578, essv15844557, essv15844591, essv15844546, essv15844564, essv15844584, essv15844562, essv15844566, essv15844545, essv15844582, essv15844574, essv15844525, essv15844548, essv15844590, essv15844586, essv15844540, essv15844554, essv15844542, essv15844531, essv15844575, essv15844522 | | Samples | NA19028, HG03559, HG03121, HG02481, HG03163, NA19914, NA18877, HG02012, HG03295, HG03193, HG02895, HG03095, HG02621, HG03452, HG03499, HG02952, NA19307, NA19119, HG03370, NA19131, NA19023, NA19457, HG02054, NA19038, HG02505, HG02281, HG01893, HG03520, HG03268, NA19317, NA18520, HG02427, NA19239, HG03055, HG03114, HG03270, HG02009, HG02943, NA19670, HG02582, NA19347, HG02449, HG02322, NA18910, HG02014, HG02537, NA19461, HG03078, NA18853, HG03571, NA19257, HG02586, NA19436, HG03064, NA19206, HG02557, NA19390, NA19256, HG03437, NA19428, HG01108, NA19818, NA18501, NA19438, HG01912, HG02646, HG03410, NA19430, HG02855, NA19312, HG01886, HG02343 | | Known Genes | | | Method | Sequencing | | Analysis | | | Platform | Multiple platforms | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_3 | | Pubmed ID | 21293372 | | Accession Number(s) | esv3642262
| | Frequency | | Sample Size | 2504 | | Observed Gain | 0 | | Observed Loss | 72 | | Observed Complex | 0 | | Frequency | n/a |
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