Variant DetailsVariant: esv2735328 Internal ID | 9969658 | Landmark | | Location Information | | Cytoband | 10p11.21 | Allele length | Assembly | Allele length | hg38 | 633 | hg19 | 633 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6904617, essv6850671, essv6799881, essv6803243, essv6935773, essv6768257, essv6731792, essv6783216, essv6695203, essv6779144, essv6768976, essv6809135, essv6952893, essv6709233, essv6827374, essv6771761, essv6919824, essv6897414, essv6970443, essv6712722, essv6681289, essv6842134, essv6944551, essv6976551, essv6912280, essv6691328, essv6787427, essv6791519, essv6702104, essv6931493, essv6968707, essv6716460 | Samples | SSM036, SSM008, SSM075, SSM064, SSM065, SSM039, SSM013, SSM009, SSM042, SSM041, SSM023, SSM028, SSM084, SSM021, SSM047, SSM069, SSM029, SSM017, SSM067, SSM086, SSM033, SSM068, SSM072, SSM020, SSM015, SSM080, SSM037, SSM070, SSM025, SSM004, SSM099, SSM043 | 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) | esv2735328
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 32 | Observed Complex | 0 | Frequency | n/a |
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