Variant DetailsVariant: esv2731545| Internal ID | 9965863 | | Landmark | | | Location Information | | | Cytoband | 6p24.3 | | Allele length | | Assembly | Allele length | | hg38 | 310 | | hg19 | 310 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv6963583, essv6723140, essv6890120, essv6865474, essv6854643, essv6808310, essv6700956, essv6860706, essv6899602, essv6848984, essv6811215, essv6837333, essv6907439 | | Samples | SSM100, SSM083, SSM027, SSM075, SSM045, SSM011, SSM097, SSM039, SSM088, SSM089, SSM014, SSM086, SSM076 | | 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) | esv2731545
| | Frequency | | Sample Size | 96 | | Observed Gain | 0 | | Observed Loss | 13 | | Observed Complex | 0 | | Frequency | n/a |
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