Variant DetailsVariant: esv2745868Internal ID | 9980152 | Landmark | | Location Information | | Cytoband | 12q13.12 | Allele length | Assembly | Allele length | hg38 | 1329 | hg19 | 1329 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6772068, essv6897667, essv6765781, essv6735202, essv6815484, essv6732148, essv6904931, essv6831324, essv6899521, essv6971551, essv6755571, essv6711221, essv6687555, essv6772067, essv6959295 | Samples | SSM065, SSM013, SSM058, SSM047, SSM026, SSM006, SSM081, SSM005, SSM077, SSM004, SSM099, SSM049, SSM063, SSM012 | Known Genes | FAIM2 | 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) | esv2745868
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 14 | Observed Complex | 0 | Frequency | n/a |
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