Variant DetailsVariant: esv2743909Internal ID | 9978193 | Landmark | | Location Information | | Cytoband | 11p15.5 | Allele length | Assembly | Allele length | hg38 | 824 | hg19 | 824 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6804177, essv6731926, essv6965468, essv6823436, essv6958956, essv6935922, essv6695349, essv6706037, essv6953024, essv6834712 | Samples | SSM027, SSM079, SSM009, SSM021, SSM047, SSM026, SSM040, SSM082, SSM037, SSM025 | Known Genes | | 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) | esv2743909
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 10 | Observed Complex | 0 | Frequency | n/a |
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