Variant DetailsVariant: esv2728040 Internal ID | 9962352 | Landmark | | Location Information | | Cytoband | 1q44 | Allele length | Assembly | Allele length | hg38 | 1080 | hg19 | 1080 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv65e201 | Supporting Variants | essv6972745, essv6937892, essv6679397, essv6781093, essv6742323, essv6697145, essv6921958, essv6801794, essv6697146, essv6669307, essv6955102, essv6914170, essv6836392, essv6950779, essv6929297, essv6675420, essv6789398, essv6821401, essv6669308, essv6961890, essv6937893, essv6853566, essv6718372, essv6679398, essv6961892, essv6878687, essv6840173, essv6825214, essv6747962, essv6961891, essv6874884, essv6910279, essv6722211, essv6710790, essv6671010, essv6840172 | Samples | SSM083, SSM027, SSM045, SSM079, SSM087, SSM038, SSM073, SSM042, SSM092, SSM084, SSM018, SSM029, SSM026, SSM032, SSM031, SSM044, SSM033, SSM068, SSM020, SSM015, SSM016, SSM053, SSM005, SSM080, SSM022, SSM070, SSM025, SSM056, SSM012 | Known Genes | | 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) | esv2728040
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 29 | Observed Complex | 0 | Frequency | n/a |
|
|