Variant DetailsVariant: esv2718897Internal ID | 9953189 | Landmark | | Location Information | | Cytoband | 19q13.42 | Allele length | Assembly | Allele length | hg38 | 150 | hg19 | 169 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv533e201 | Supporting Variants | essv6674864, essv6868472, essv6678907, essv6797174, essv6804250, essv6820943, essv6703601, essv6852867, essv6863677 | Samples | SSM071, SSM039, SSM073, SSM088, SSM089, SSM032, SSM031, SSM086, SSM078 | Known Genes | | 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) | esv2718897
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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