Variant DetailsVariant: esv2728017 Internal ID | 9962329 | Landmark | | Location Information | | Cytoband | 1q44 | Allele length | Assembly | Allele length | hg38 | 58034 | hg19 | 58034 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6972745, essv6729836, essv6937892, essv6679397, essv6781093, essv6785216, essv6742323, essv6697145, essv6769751, essv6886155, essv6829203, essv6704048, essv6921958, essv6836393, essv6847368, essv6968175, essv6801794, essv6707461, essv6710791, essv6697146, essv6669307, essv6750487, essv6825213, essv6773658, essv6840171, essv6955102, essv6756705, essv6914170, essv6714461, essv6836392, essv6950779, essv6929297, essv6925882, essv6968172, essv6693018, essv6675420, essv6955101, essv6892523, essv6789398, essv6801793, essv6853565, essv6933538, essv6902746, essv6883419, essv6950780, essv6896016, essv6720531, essv6844063, essv6933537, essv6889209, essv6821401, essv6810505, essv6821402, essv6739023, essv6669308, essv6968173, essv6726069, essv6961890, essv6813357, essv6813358, essv6816853, essv6797693, essv6937893, essv6929295, essv6853566, essv6718372, essv6679398, essv6914169, essv6889211, essv6847369, essv6961892, essv6683016, essv6797694, essv6878687, essv6845787, essv6840173, essv6825214, essv6871892, essv6747962, essv6781094, essv6961891, essv6874884, essv6777145, essv6910279, essv6742324, essv6722211, essv6710790, essv6671010, essv6840172 | Samples | SSM059, SSM008, SSM083, SSM027, SSM045, SSM046, SSM011, SSM079, SSM065, SSM087, SSM038, SSM097, SSM013, SSM073, SSM042, SSM041, SSM028, SSM092, SSM084, SSM021, SSM047, SSM018, SSM069, SSM029, SSM096, SSM026, SSM019, SSM032, SSM031, SSM067, SSM044, SSM086, SSM033, SSM066, SSM085, SSM068, SSM081, SSM040, SSM072, SSM020, SSM007, SSM015, SSM078, SSM016, SSM053, SSM005, SSM080, SSM037, SSM077, SSM076, SSM022, SSM091, SSM070, SSM095, SSM025, SSM034, SSM099, SSM043, SSM052, SSM098, SSM056, SSM012 | Known Genes | OR2M2, OR2M3, OR2M5 | Method | Sequencing | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads | Platform | Illumina HiSeq 2000 | Comments | | Reference | Wong_et_al_2012b | Pubmed ID | 23290073 | Accession Number(s) | esv2728017
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 62 | Observed Complex | 0 | Frequency | n/a |
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