Variant DetailsVariant: esv2746226Internal ID | 9980510 | Landmark | | Location Information | | Cytoband | 12q22 | Allele length | Assembly | Allele length | hg38 | 328 | hg19 | 328 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6806422, essv6720740, essv6787809, essv6819760, essv6851275, essv6866176, essv6834933, essv6857281, essv6908937, essv6800268, essv6702506, essv6965855, essv6927972 | Samples | SSM027, SSM011, SSM087, SSM039, SSM074, SSM069, SSM019, SSM044, SSM014, SSM086, SSM072, SSM082, SSM078 | Known Genes | PLXNC1 | 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) | esv2746226
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
|
|