Variant DetailsVariant: dgv96e201Internal ID | 20124983 | Landmark | | Location Information | | Cytoband | 10p11.21 | Allele length | Assembly | Allele length | hg38 | 553 | hg19 | 553 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | esv2735350, esv2735339 | Samples | SSM065, SSM039, SSM013, SSM042, SSM041, SSM023, SSM084, SSM021, SSM069, SSM017, SSM067, SSM086, SSM033, SSM068, SSM080, SSM070, SSM004, SSM099 | Known Genes | CREM | 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) | dgv96e201
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 18 | Observed Complex | 0 | Frequency | n/a |
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