Variant DetailsVariant: esv2723552Internal ID | 9957852 | Landmark | | Location Information | | Cytoband | 21q22.3 | Allele length | Assembly | Allele length | hg38 | 929 | hg19 | 929 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6961380, essv6859084, essv6967808, essv6689196, essv6666820, essv6921630, essv6821097 | Samples | SSM027, SSM087, SSM029, SSM026, SSM017, SSM035, SSM078 | Known Genes | SLC37A1 | 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) | esv2723552
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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