Variant DetailsVariant: dgv455e201| Internal ID | 20125342 | | Landmark | | | Location Information | | | Cytoband | 18q21.2 | | Allele length | | Assembly | Allele length | | hg38 | 456 | | hg19 | 456 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | esv2717131, esv2717132 | | Samples | SSM087, SSM039, SSM026, SSM017, SSM032, SSM031, SSM014, SSM086, SSM072, SSM015 | | Known Genes | TCF4 | | 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) | dgv455e201
| | Frequency | | Sample Size | 96 | | Observed Gain | 0 | | Observed Loss | 10 | | Observed Complex | 0 | | Frequency | n/a |
|
|