Variant DetailsVariant: esv2729464Internal ID | 9963779 | Landmark | | Location Information | | Cytoband | 5p15.33 | Allele length | Assembly | Allele length | hg38 | 739 | hg19 | 739 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6748502, essv6893229, essv6885542, essv6670653, essv6875468, essv6822182, essv6693868, essv6701832, essv6736730, essv6963224, essv6934389, essv6969061, essv6963225, essv6817825 | Samples | SSM027, SSM079, SSM050, SSM028, SSM092, SSM021, SSM031, SSM006, SSM078, SSM037, SSM098, SSM056, SSM012 | Known Genes | TERT | 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) | esv2729464
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
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