Variant DetailsVariant: esv2745277Internal ID | 9979561 | Landmark | | Location Information | | Cytoband | 11q25 | Allele length | Assembly | Allele length | hg38 | 284 | hg19 | 284 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6977071, essv6819639, essv6834835, essv6771999, essv6668180, essv6912535 | Samples | SSM065, SSM029, SSM082, SSM015, SSM078, SSM030 | Known Genes | NTM | 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) | esv2745277
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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