Variant DetailsVariant: esv3636024 Internal ID | 6676133 | Landmark | | Location Information | | Cytoband | 15q13.2 | Allele length | Assembly | Allele length | hg38 | 469178 | hg19 | 469178 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15203546, essv15203564, essv15203601, essv15203565, essv15203603, essv15203575, essv15203554, essv15203594, essv15203515, essv15203604, essv15203573, essv15203556, essv15203597, essv15203591, essv15203605, essv15203589, essv15203585, essv15203596, essv15203551, essv15203563, essv15203545, essv15203527, essv15203516, essv15203560, essv15203607, essv15203518, essv15203540, essv15203520, essv15203615, essv15203547, essv15203537, essv15203522, essv15203552, essv15203588, essv15203536, essv15203532, essv15203574, essv15203610, essv15203576, essv15203587, essv15203621, essv15203555, essv15203541, essv15203549, essv15203569, essv15203617, essv15203542, essv15203571, essv15203599, essv15203528, essv15203521, essv15203535, essv15203530, essv15203614, essv15203600, essv15203620, essv15203580, essv15203526, essv15203584, essv15203619, essv15203517, essv15203570, essv15203578, essv15203524, essv15203598, essv15203595, essv15203539, essv15203533, essv15203613, essv15203606, essv15203582, essv15203592, essv15203616, essv15203568, essv15203593, essv15203579, essv15203618, essv15203550, essv15203548, essv15203557, essv15203523, essv15203583, essv15203609, essv15203611, essv15203562, essv15203572, essv15203602, essv15203586, essv15203581, essv15203538, essv15203561, essv15203519, essv15203622, essv15203590, essv15203525, essv15203529, essv15203531, essv15203608, essv15203553, essv15203543, essv15203544, essv15203558, essv15203612, essv15203567, essv15203559, essv15203534, essv15203577, essv15203566 | Samples | HG03096, NA21110, HG02628, HG03121, NA19397, HG01462, NA19909, NA19399, HG02433, HG03517, NA11920, HG03057, HG03607, HG03449, HG02798, NA18603, NA18486, NA20294, HG03518, NA18870, HG03679, NA18510, NA19107, HG03199, NA19201, HG03499, HG02325, NA18916, NA11992, NA19023, HG03578, NA18498, HG03479, HG02922, HG03079, HG01893, HG03556, HG02573, NA19917, HG02461, NA19207, HG03195, HG03225, HG03073, NA19025, HG03270, HG03169, HG02716, HG02943, NA19247, NA18934, NA19175, NA19152, HG01271, HG03547, NA19184, HG02449, HG02322, NA18516, NA18915, HG02144, NA18871, HG02497, HG02470, HG01889, HG02757, HG03136, NA19042, HG03397, HG02884, NA19099, HG02256, NA19756, NA18523, HG03109, NA19436, NA20296, NA19375, HG02330, HG02684, NA18909, HG03437, HG02799, HG03367, NA19454, NA18950, HG03689, HG02611, HG02314, HG02982, HG03473, HG01137, NA20887, NA19818, HG03565, HG03442, NA19223, HG03025, HG02938, NA19102, NA19096, NA19711, HG03470, NA19900, HG01883, HG02006, HG01061, NA19153 | Known Genes | CHRFAM7A, DKFZP434L187, GOLGA8J, GOLGA8T, LOC101059918, ULK4P3 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3636024
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 108 | Observed Complex | 0 | Frequency | n/a |
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