Variant DetailsVariant: esv2726485 Internal ID | 9960792 | Landmark | | Location Information | | Cytoband | 1q43 | Allele length | Assembly | Allele length | hg38 | 585 | hg19 | 585 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6910257, essv6750287, essv6968153, essv6710770, essv6918473, essv6917638, essv6942012, essv6804582, essv6821385, essv6729818, essv6773640, essv6785193, essv6699820, essv6753677, essv6937870, essv6669278, essv6679375, essv6929273, essv6840148 | Samples | SSM008, SSM079, SSM039, SSM074, SSM042, SSM023, SSM058, SSM028, SSM084, SSM047, SSM069, SSM017, SSM003, SSM031, SSM033, SSM066, SSM020, SSM015, SSM022 | Known Genes | SDCCAG8 | 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) | esv2726485
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 19 | Observed Complex | 0 | Frequency | n/a |
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