Variant DetailsVariant: esv2743932Internal ID | 9978216 | Landmark | | Location Information | | Cytoband | 11p15.5 | Allele length | Assembly | Allele length | hg38 | 147 | hg19 | 147 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6940123, essv6856901, essv6724307, essv6850871, essv6681408, essv6919968, essv6904732, essv6819470, essv6900485 | Samples | SSM100, SSM045, SSM087, SSM013, SSM017, SSM086, SSM033, SSM078, SSM022 | Known Genes | BRSK2 | 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) | esv2743932
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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