Variant DetailsVariant: esv2731275Internal ID | 9965592 | Landmark | | Location Information | | Cytoband | 5q35.3 | Allele length | Assembly | Allele length | hg38 | 485 | hg19 | 485 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6700930, essv6903617, essv6943241, essv6927118, essv6833662, essv6951756, essv6730766, essv6694035, essv6922940, essv6778064, essv6708310 | Samples | SSM039, SSM013, SSM041, SSM023, SSM047, SSM018, SSM003, SSM067, SSM082, SSM037, SSM025 | Known Genes | ADAMTS2 | 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) | esv2731275
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 11 | Observed Complex | 0 | Frequency | n/a |
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