Variant DetailsVariant: esv3588060 | Internal ID | 6975484 | | Landmark | | | Location Information | | | Cytoband | 1q25.2 | | Allele length | | Assembly | Allele length | | hg38 | 1403 | | hg19 | 1403 |
| | Variant Type | CNV loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv10200124, essv10200100, essv10200077, essv10200098, essv10200084, essv10200125, essv10200136, essv10200116, essv10200129, essv10200086, essv10200073, essv10200123, essv10200118, essv10200092, essv10200121, essv10200104, essv10200085, essv10200134, essv10200081, essv10200076, essv10200105, essv10200069, essv10200106, essv10200080, essv10200115, essv10200091, essv10200114, essv10200137, essv10200117, essv10200107, essv10200108, essv10200094, essv10200132, essv10200078, essv10200079, essv10200119, essv10200110, essv10200075, essv10200095, essv10200122, essv10200096, essv10200087, essv10200113, essv10200133, essv10200090, essv10200103, essv10200068, essv10200111, essv10200083, essv10200101, essv10200138, essv10200131, essv10200093, essv10200120, essv10200126, essv10200089, essv10200139, essv10200130, essv10200088, essv10200070, essv10200112, essv10200099, essv10200127, essv10200071, essv10200097, essv10200128, essv10200082, essv10200135, essv10200109, essv10200074, essv10200072, essv10200102 | | Samples | HG03228, NA12286, HG01438, NA11995, HG04229, NA21092, HG00306, HG02600, NA19777, HG00150, HG01632, HG02688, HG04001, NA12155, NA12413, NA12341, HG01779, HG01488, HG00173, NA20756, HG01710, HG03762, HG01069, HG02490, HG01757, HG04106, HG03777, NA21107, HG01259, HG00338, NA20753, HG02737, HG01784, HG03908, HG00145, NA12342, HG04062, HG00190, NA20521, HG04107, HG01088, HG01498, NA20767, NA20876, NA20525, HG03858, NA20881, HG00140, NA19752, NA06985, HG03774, HG00240, HG00126, HG00366, HG02682, HG00357, HG04003, NA19818, HG01606, HG02694, HG00381, HG01783, HG00174, HG04098, HG02681, HG00274, NA11892, HG01082, NA12154, NA20908, HG01786, HG00553 | | Known Genes | | | Method | Sequencing | | Analysis | | | Platform | Multiple platforms | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_3 | | Pubmed ID | 21293372 | | Accession Number(s) | esv3588060
| | Frequency | | Sample Size | 2504 | | Observed Gain | 0 | | Observed Loss | 72 | | Observed Complex | 0 | | Frequency | n/a |
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