Variant DetailsVariant: esv3646133 Internal ID | 6686192 | Landmark | | Location Information | | Cytoband | 20q13.2 | Allele length | Assembly | Allele length | hg38 | 11031 | hg19 | 11031 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv16206110, essv16206060, essv16206119, essv16206036, essv16206040, essv16206127, essv16206072, essv16206083, essv16206095, essv16206111, essv16206048, essv16206082, essv16206039, essv16206091, essv16206103, essv16206081, essv16206086, essv16206058, essv16206100, essv16206099, essv16206046, essv16206061, essv16206043, essv16206122, essv16206041, essv16206104, essv16206033, essv16206028, essv16206093, essv16206121, essv16206056, essv16206076, essv16206052, essv16206038, essv16206117, essv16206089, essv16206059, essv16206067, essv16206128, essv16206074, essv16206053, essv16206112, essv16206106, essv16206047, essv16206080, essv16206044, essv16206029, essv16206027, essv16206114, essv16206092, essv16206054, essv16206120, essv16206105, essv16206031, essv16206108, essv16206090, essv16206096, essv16206071, essv16206068, essv16206118, essv16206057, essv16206034, essv16206107, essv16206116, essv16206113, essv16206064, essv16206126, essv16206049, essv16206085, essv16206109, essv16206070, essv16206037, essv16206050, essv16206066, essv16206115, essv16206125, essv16206073, essv16206051, essv16206101, essv16206032, essv16206079, essv16206035, essv16206045, essv16206030, essv16206065, essv16206075, essv16206088, essv16206084, essv16206069, essv16206124, essv16206063, essv16206102, essv16206062, essv16206094, essv16206087, essv16206055, essv16206078, essv16206098, essv16206042, essv16206123, essv16206077, essv16206097 | Samples | NA12383, HG01485, HG00114, HG01746, NA19648, HG01173, NA19794, HG00102, HG00351, NA20783, HG01079, NA20878, NA19704, HG01280, NA20531, HG01374, HG00640, NA21115, HG03126, HG00737, HG00150, HG01140, HG01070, HG03757, NA20850, HG02105, HG02485, HG01997, NA20756, HG01459, HG04182, HG03246, HG02603, NA12275, HG01067, HG02490, HG01757, HG00637, NA20764, HG01550, NA20515, HG01124, HG01353, HG01136, HG00188, HG00731, HG01360, HG00380, NA20524, HG00332, NA12878, HG01095, HG00368, HG03900, HG00275, NA20506, HG01345, NA20832, NA20767, NA20770, HG01073, NA21124, NA21141, HG04173, HG01474, HG00146, NA19682, NA20828, HG02635, HG00240, NA21142, HG04093, HG01956, NA20534, HG01257, NA21087, HG03598, NA21117, HG01190, HG00366, NA20815, HG00375, HG01174, HG03850, HG02982, NA19467, NA20887, NA19818, NA19759, HG03789, HG02970, NA20582, HG01089, NA19185, HG02768, HG01468, NA19661, HG01431, HG01125, HG04161, NA20827, HG01191 | Known Genes | BCAS1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3646133
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 102 | Observed Complex | 0 | Frequency | n/a |
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