Variant DetailsVariant: dgv130e201Internal ID | 20125017 | Landmark | | Location Information | | Cytoband | 11p15.5 | Allele length | Assembly | Allele length | hg38 | 371 | hg19 | 371 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | esv2743923, esv2743925 | Samples | SSM008, SSM027, SSM097, SSM050, SSM074, SSM028, SSM090, SSM019, SSM094, SSM044, SSM085, SSM081, SSM015, SSM078, SSM077, SSM055, SSM095, SSM099, SSM043, SSM098, SSM056, SSM012 | 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) | dgv130e201
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 22 | Observed Complex | 0 | Frequency | n/a |
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