Variant DetailsVariant: esv2747351Internal ID | 9981635 | Landmark | | Location Information | | Cytoband | 13q14.13 | Allele length | Assembly | Allele length | hg38 | 1500 | hg19 | 1500 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6809499, essv6966044, essv6720829, essv6835965, essv6940340, essv6873796, essv6928053 | Samples | SSM027, SSM075, SSM019, SSM003, SSM044, SSM010, SSM091 | 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) | esv2747351
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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