Variant DetailsVariant: nsv554895 Internal ID | 15995618 | Landmark | | Location Information | | Cytoband | 11q11 | Allele length | Assembly | Allele length | hg38 | 71348 | hg19 | 71348 | hg18 | 71348 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv1915n54 | Supporting Variants | nssv1175156, nssv1175101, nssv1175165, nssv1175132, nssv1175187, nssv1175095, nssv1175154, nssv1175162, nssv1175123, nssv1175175, nssv1175110, nssv1175174, nssv1175122, nssv1175131, nssv1175116, nssv1175184, nssv1175098, nssv1175146, nssv1175138, nssv1175160, nssv1175144, nssv776023, nssv1175115, nssv1175111, nssv1175167, nssv1175094, nssv1175177, nssv1175183, nssv1175178, nssv1175136, nssv1175118, nssv1175109, nssv1175126, nssv1175124, nssv1175155, nssv1175157, nssv1175191, nssv776022, nssv1175121, nssv1175093, nssv1175119, nssv1175159, nssv1175141, nssv1175161, nssv1175107, nssv1175134, nssv1175129, nssv1175149, nssv1175143, nssv1175142, nssv1175176, nssv1175192, nssv1175182, nssv1175169, nssv1175188, nssv776020, nssv1175137, nssv1175127, nssv1175180, nssv1175097, nssv1175152, nssv1175164, nssv1175179, nssv1175171, nssv1175114, nssv1175189, nssv1175108, nssv1175106, nssv1175185, nssv1175145, nssv1175147, nssv1175190, nssv1175153, nssv1175139, nssv1175150, nssv776021, nssv1175103, nssv1175163, nssv1175100, nssv1175099, nssv1175096, nssv1175158, nssv1175173, nssv1175117, nssv1175172, nssv1175128, nssv1175125, nssv1175105, nssv1175113, nssv1175104, nssv1175102, nssv1175186, nssv1175148, nssv1175130, nssv1175120, nssv1175170, nssv1175140, nssv1175133, nssv1175112, nssv1175166, nssv1175135, nssv1175181, nssv1175168, nssv1175151 | Samples | HGDP01209, HGDP00997, HGDP01208, NINDS_163, HGDP00958, HGDP01212, HGDP00277, HGDP00621, HGDP00445, HGDP00315, HGDP01234, HGDP00627, HGDP01231, HGDP00995, HGDP00195, HGDP00814, HGDP00113, HGDP01281, HGDP00772, HGDP00088, 1780854257_A, HGDP01384, HGDP00258, HGDP01191, HGDP00755, HGDP00631, HGDP01010, HGDP00140, HGDP00679, HGDP01004, HGDP01049, HGDP00136, HGDP01274, HGDP00286, HGDP01048, HGDP00066, HGDP01040, HGDP00959, HGDP00760, HGDP01287, HGDP01037, HGDP00891, HGDP00150, HGDP00526, HGDP00952, HGDP01279, HGDP00633, HGDP01268, HGDP00848, HGDP00112, HGDP00522, HGDP01096, HGDP00778, HGDP01320, HGDP00980, HGDP00237, HGDP01338, 1780862416_A, HGDP00747, HGDP01012, HGDP00761, HGDP01273, HGDP00438, HGDP00676, 1780862160_A, HGDP00121, HGDP01307, HGDP00928, HGDP01362, HGDP01099, NINDS_65, HGDP01097, HGDP01198, HGDP00351, HGDP00309, HGDP00886, HGDP00793, HGDP01319, HGDP01400, HGDP00158, HGDP01351, HGDP01374, HGDP01077, HGDP01179, HGDP00877, HGDP01327, HGDP01157, HGDP01226, HGDP00736, HGDP01180, HGDP00239, HGDP00319, HGDP00819, HGDP00336, HGDP00876, HGDP01011, HGDP00155, HGDP00914, HGDP00544, HGDP00616 | Known Genes | OR4C11, OR4C6, OR4P4, OR4S2 | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | nsv554895
| Frequency | Sample Size | 17421 | Observed Gain | 9 | Observed Loss | 95 | Observed Complex | 0 | Frequency | n/a |
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