Variant DetailsVariant: esv2728143Internal ID | 9962456 | Landmark | | Location Information | | Cytoband | 4q25 | 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 | essv6865061, essv6889795, essv6848416, essv6962966, essv6973964, essv6907042, essv6704623, essv6670402, essv6700569, essv6854555, essv6899340, essv6686882, essv6855265, essv6825947, essv6956256, essv6708028, essv6851797, essv6817647, essv6860274 | Samples | SSM100, SSM027, SSM011, SSM087, SSM097, SSM039, SSM088, SSM002, SSM041, SSM029, SSM026, SSM089, SSM035, SSM031, SSM014, SSM086, SSM040, SSM078, SSM080 | Known Genes | | 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) | esv2728143
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 19 | Observed Complex | 0 | Frequency | n/a |
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