Variant DetailsVariant: esv3637503 | Internal ID | 7024295 | | Landmark | | | Location Information | | | Cytoband | 15q26.3 | | Allele length | | Assembly | Allele length | | hg38 | 2913 | | hg19 | 2913 |
| | Variant Type | CNV loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv15354237, essv15354257, essv15354142, essv15354249, essv15354171, essv15354240, essv15354222, essv15354188, essv15354182, essv15354169, essv15354207, essv15354143, essv15354259, essv15354239, essv15354253, essv15354159, essv15354260, essv15354272, essv15354200, essv15354177, essv15354275, essv15354148, essv15354245, essv15354251, essv15354217, essv15354262, essv15354172, essv15354238, essv15354250, essv15354202, essv15354265, essv15354185, essv15354271, essv15354193, essv15354191, essv15354186, essv15354252, essv15354268, essv15354198, essv15354256, essv15354209, essv15354203, essv15354224, essv15354264, essv15354227, essv15354258, essv15354235, essv15354157, essv15354136, essv15354197, essv15354141, essv15354137, essv15354153, essv15354244, essv15354150, essv15354180, essv15354220, essv15354212, essv15354145, essv15354160, essv15354214, essv15354205, essv15354228, essv15354175, essv15354277, essv15354215, essv15354154, essv15354261, essv15354236, essv15354147, essv15354211, essv15354139, essv15354221, essv15354225, essv15354163, essv15354174, essv15354162, essv15354165, essv15354140, essv15354269, essv15354276, essv15354189, essv15354273, essv15354199, essv15354195, essv15354179, essv15354194, essv15354187, essv15354181, essv15354216, essv15354161, essv15354164, essv15354243, essv15354213, essv15354167, essv15354247, essv15354166, essv15354241, essv15354204, essv15354170, essv15354151, essv15354168, essv15354231, essv15354144, essv15354274, essv15354263, essv15354242, essv15354219, essv15354223, essv15354176, essv15354232, essv15354178, essv15354155, essv15354146, essv15354183, essv15354149, essv15354201, essv15354248, essv15354138, essv15354246, essv15354229, essv15354152, essv15354190, essv15354158, essv15354184, essv15354266, essv15354210, essv15354208, essv15354254, essv15354218, essv15354206, essv15354226, essv15354192, essv15354255, essv15354233, essv15354156, essv15354173, essv15354230, essv15354267, essv15354234, essv15354270, essv15354196 | | Samples | HG00403, HG01060, HG01441, HG00542, HG00442, HG02610, NA20529, HG01918, HG01443, NA19664, HG01961, NA19066, HG01359, HG00559, HG01052, NA18980, HG02262, NA18561, HG01374, HG02836, HG03115, HG01465, HG00699, HG03926, HG00566, NA18959, NA19669, HG03172, HG01051, HG01350, HG00589, HG01853, HG02541, NA18635, NA18567, NA18558, HG02266, HG01945, HG01492, NA11992, HG03246, HG03105, NA19023, NA19054, HG01840, NA19681, HG01982, HG01859, HG01893, NA19720, HG01080, HG03189, HG01849, HG01369, NA18748, NA19172, HG00705, HG01973, HG01932, NA19725, HG01198, NA18557, HG02260, HG01133, HG03267, NA18975, HG00419, NA18539, NA18638, HG00675, HG00464, HG01565, NA18645, HG03343, HG01139, NA18605, NA18538, HG01501, HG01595, HG00653, NA19455, HG01979, HG00584, HG02390, HG00500, HG02102, HG01323, HG00619, HG01948, NA18548, NA18566, HG01102, NA18573, HG00690, HG00531, NA19042, HG01921, HG03634, HG03046, HG01474, HG00704, HG01936, NA18531, HG01204, NA18646, NA18974, HG01257, HG03064, HG01858, HG00611, NA18632, NA20522, NA18543, HG02799, NA19735, HG04186, HG00580, HG01623, NA18992, HG01205, NA19439, HG02274, NA19085, HG00707, HG01577, HG01770, HG00478, HG01491, HG00409, HG03025, NA20852, HG01872, HG02348, NA19661, HG01111, HG01082, HG02425, HG02406, NA19074, NA20509, HG01926, HG00593 | | Known Genes | CHSY1 | | Method | Sequencing | | Analysis | | | Platform | Multiple platforms | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_3 | | Pubmed ID | 21293372 | | Accession Number(s) | esv3637503
| | Frequency | | Sample Size | 2504 | | Observed Gain | 0 | | Observed Loss | 142 | | Observed Complex | 0 | | Frequency | n/a |
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