Variant DetailsVariant: esv3636557 | Internal ID | 7023351 | | Landmark | | | Location Information | | | Cytoband | 15q21.3 | | Allele length | | Assembly | Allele length | | hg38 | 3097 | | hg19 | 3097 |
| | Variant Type | CNV loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv15255746, essv15255736, essv15255724, essv15255705, essv15255753, essv15255777, essv15255781, essv15255723, essv15255759, essv15255669, essv15255764, essv15255793, essv15255716, essv15255691, essv15255748, essv15255745, essv15255727, essv15255667, essv15255696, essv15255713, essv15255725, essv15255685, essv15255770, essv15255788, essv15255749, essv15255726, essv15255771, essv15255692, essv15255763, essv15255657, essv15255784, essv15255768, essv15255734, essv15255761, essv15255778, essv15255792, essv15255790, essv15255757, essv15255661, essv15255751, essv15255762, essv15255738, essv15255722, essv15255783, essv15255707, essv15255702, essv15255672, essv15255739, essv15255774, essv15255684, essv15255747, essv15255787, essv15255668, essv15255720, essv15255767, essv15255750, essv15255671, essv15255673, essv15255706, essv15255695, essv15255740, essv15255674, essv15255697, essv15255732, essv15255712, essv15255682, essv15255701, essv15255765, essv15255752, essv15255776, essv15255785, essv15255708, essv15255741, essv15255703, essv15255711, essv15255663, essv15255678, essv15255709, essv15255690, essv15255744, essv15255715, essv15255758, essv15255728, essv15255730, essv15255769, essv15255737, essv15255683, essv15255699, essv15255780, essv15255779, essv15255731, essv15255689, essv15255666, essv15255680, essv15255675, essv15255755, essv15255687, essv15255786, essv15255742, essv15255789, essv15255700, essv15255686, essv15255679, essv15255660, essv15255718, essv15255698, essv15255710, essv15255717, essv15255733, essv15255677, essv15255719, essv15255662, essv15255729, essv15255694, essv15255665, essv15255721, essv15255766, essv15255688, essv15255681, essv15255754, essv15255670, essv15255704, essv15255693, essv15255775, essv15255794, essv15255735, essv15255772, essv15255756, essv15255743, essv15255664, essv15255791, essv15255760, essv15255658, essv15255676, essv15255714, essv15255659, essv15255782, essv15255773 | | Samples | NA18745, HG03812, HG03652, HG03965, HG01624, HG03237, HG01860, NA20274, HG01815, HG00766, HG04202, HG03738, HG02061, HG01802, NA19057, HG02050, HG01944, NA18959, NA18606, NA19669, HG00879, HG02023, HG01809, HG00717, NA19089, NA19076, NA21135, NA18550, HG02151, HG01682, HG02690, HG02407, NA18595, HG03808, HG00689, HG00674, HG04206, NA18567, HG02687, NA20911, NA18619, HG00458, HG03913, HG01599, NA18960, NA18942, HG01816, NA18582, NA18964, HG03917, NA19079, NA18949, HG03594, HG00590, NA18749, HG04183, HG00683, NA21109, NA18977, NA12815, NA20889, HG01058, HG01709, NA19445, HG00178, NA18954, HG00419, HG02164, NA18544, HG02136, NA19091, NA19070, NA19006, HG02513, HG01247, HG01857, HG01104, NA19077, HG00701, HG00584, NA19081, HG04019, HG02522, NA18976, HG02221, NA19064, NA18537, NA18566, NA20867, HG01619, NA20903, NA19084, HG00956, HG00479, NA19001, HG02283, HG03971, NA18945, NA21113, NA18542, HG03866, HG04188, NA18543, NA19072, HG03949, HG03689, HG01396, HG01866, HG04099, NA18643, HG01137, NA19083, HG04090, NA19085, NA18610, HG00620, NA20888, NA20897, HG00614, HG01432, NA20868, HG02238, HG00421, HG02396, HG02116, NA21093, NA18609, HG03615, HG00274, NA18957, HG02028, HG01863, NA18968, NA19065, NA18549, HG03686, NA18562, NA18577 | | Known Genes | CCPG1, DYX1C1-CCPG1 | | Method | Sequencing | | Analysis | | | Platform | Multiple platforms | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_3 | | Pubmed ID | 21293372 | | Accession Number(s) | esv3636557
| | Frequency | | Sample Size | 2504 | | Observed Gain | 0 | | Observed Loss | 138 | | Observed Complex | 0 | | Frequency | n/a |
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