Variant DetailsVariant: esv2729851Internal ID | 9964166 | Landmark | | Location Information | | Cytoband | 10p15.3 | Allele length | Assembly | Allele length | hg38 | 463 | hg19 | 463 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6970387, essv6958620, essv6803225, essv6897365, essv6948672, essv6823270, essv6705877, essv6731744, essv6850579, essv6968318, essv6783157, essv6724137, essv6931432, essv6856609 | Samples | SSM024, SSM045, SSM079, SSM087, SSM073, SSM028, SSM047, SSM026, SSM086, SSM068, SSM040, SSM020, SSM004, SSM099 | Known Genes | ADARB2 | 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) | esv2729851
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 14 | Observed Complex | 0 | Frequency | n/a |
|
|