Variant DetailsVariant: esv2723611 Internal ID | 9957911 | Landmark | | Location Information | | Cytoband | 21q22.3 | Allele length | Assembly | Allele length | hg38 | 578 | hg19 | 578 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6917344, essv6824890, essv6776842, essv6954609, essv6961388, essv6797358, essv6946401, essv6928983, essv6714156, essv6902451, essv6843813, essv6780767, essv6941693, essv6682767, essv6937583, essv6967815, essv6921635, essv6972213, essv6666830, essv6773360, essv6816507, essv6950454, essv6832502, essv6784897, essv6853118, essv6925613, essv6859093, essv6769438, essv6816209, essv6733425, essv6801552 | Samples | SSM071, SSM027, SSM024, SSM064, SSM079, SSM065, SSM087, SSM009, SSM042, SSM023, SSM028, SSM084, SSM021, SSM047, SSM018, SSM029, SSM026, SSM017, SSM019, SSM067, SSM086, SSM033, SSM066, SSM068, SSM081, SSM072, SSM016, SSM077, SSM022, SSM025, SSM012 | Known Genes | HSF2BP | 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) | esv2723611
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 31 | Observed Complex | 0 | Frequency | n/a |
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