Variant DetailsVariant: esv2730273Internal ID | 9964589 | Landmark | | Location Information | | Cytoband | 10p15.3 | Allele length | Assembly | Allele length | hg38 | 467 | hg19 | 467 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6791469, essv6866667, essv6935963, essv6830960, essv6887716, essv6850588, essv6705879, essv6894337, essv6850587, essv6724141, essv6731745, essv6948679, essv6799840, essv6702051, essv6897367 | Samples | SSM024, SSM045, SSM039, SSM047, SSM096, SSM089, SSM003, SSM086, SSM081, SSM040, SSM072, SSM070, SSM099, SSM098 | 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) | esv2730273
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 14 | Observed Complex | 0 | Frequency | n/a |
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