Variant DetailsVariant: dgv150e201Internal ID | 20125037 | Landmark | | Location Information | | Cytoband | 11q24.2 | Allele length | Assembly | Allele length | hg38 | 644 | hg19 | 644 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | esv2745199, esv2745196 | Samples | SSM045, SSM064, SSM084, SSM021, SSM026, SSM067, SSM086, SSM066, SSM068, SSM081, SSM020, SSM070, SSM034, SSM043 | Known Genes | PKNOX2 | 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) | dgv150e201
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 14 | Observed Complex | 0 | Frequency | n/a |
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