Variant DetailsVariant: esv3625335![](http://dgv.tcag.ca/gb2/gbrowse_img/dgv2_hg38/?name=chr11:9482211..9487582;width=800;overview=1) Internal ID | 6665482 | Landmark | | Location Information | | Cytoband | 11p15.4 | Allele length | Assembly | Allele length | hg38 | 5372 | hg19 | 5372 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv14023766, essv14023749, essv14023769, essv14023688, essv14023768, essv14023729, essv14023733, essv14023709, essv14023705, essv14023731, essv14023760, essv14023763, essv14023734, essv14023703, essv14023758, essv14023687, essv14023740, essv14023708, essv14023745, essv14023764, essv14023718, essv14023698, essv14023726, essv14023770, essv14023725, essv14023720, essv14023706, essv14023695, essv14023737, essv14023722, essv14023716, essv14023750, essv14023712, essv14023692, essv14023767, essv14023724, essv14023753, essv14023697, essv14023730, essv14023739, essv14023765, essv14023711, essv14023738, essv14023735, essv14023715, essv14023746, essv14023759, essv14023747, essv14023751, essv14023732, essv14023682, essv14023693, essv14023771, essv14023774, essv14023701, essv14023710, essv14023736, essv14023719, essv14023699, essv14023690, essv14023700, essv14023757, essv14023727, essv14023773, essv14023704, essv14023752, essv14023755, essv14023684, essv14023728, essv14023762, essv14023741, essv14023717, essv14023689, essv14023742, essv14023686, essv14023721, essv14023744, essv14023754, essv14023702, essv14023756, essv14023743, essv14023748, essv14023685, essv14023723, essv14023683, essv14023694, essv14023714, essv14023696, essv14023691, essv14023713, essv14023772, essv14023761, essv14023707, essv14023681 | Samples | NA19394, NA18502, HG02890, HG02944, HG02628, HG02583, HG03163, HG01052, NA18507, HG02852, HG02891, HG02870, HG03280, NA19355, HG03515, HG02589, NA19190, NA19920, HG02895, HG03464, NA19379, HG02621, NA19448, NA19307, HG03091, HG02595, HG02645, NA19197, HG03578, HG03224, HG02703, HG03556, NA18874, HG02573, NA19917, NA19238, NA19024, HG02885, NA19172, NA19471, NA18908, HG03048, HG02977, NA19908, NA19984, HG02449, HG02253, HG01882, HG03457, NA19982, NA18910, HG02470, HG03124, HG01092, HG03301, NA18879, HG02309, NA19320, HG03024, NA19099, HG02979, NA18523, HG02635, HG02594, HG02484, HG03064, NA19256, HG03437, NA19434, NA19037, HG03127, NA19439, HG02941, NA19310, HG03473, HG02464, HG02580, HG02814, HG03103, NA19351, HG02646, HG02053, HG03060, HG02462, HG01914, HG02947, HG02465, NA19463, HG01886, HG02808, HG03118, HG00553, NA19153, HG03265 | Known Genes | ZNF143 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3625335
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 94 | Observed Complex | 0 | Frequency | n/a |
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