Variant DetailsVariant: esv2746357Internal ID | 9980641 | Landmark | | Location Information | | Cytoband | 12q24.12 | Allele length | Assembly | Allele length | hg38 | 407 | hg19 | 407 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6904965, essv6862471, essv6695616, essv6691666, essv6866320, essv6772731, essv6755623, essv6724560 | Samples | SSM036, SSM008, SSM045, SSM011, SSM013, SSM088, SSM058, SSM037 | Known Genes | CUX2 | 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) | esv2746357
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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