Variant DetailsVariant: esv2731363Internal ID | 9965680 | Landmark | | Location Information | | Cytoband | 6p25.3 | Allele length | Assembly | Allele length | hg38 | 751 | hg19 | 751 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6878524, essv6680294, essv6670962, essv6963543, essv6943484, essv6907420, essv6837316, essv6890102, essv6727027, essv6676437, essv6865451, essv6884123, essv6711725, essv6918631, essv6694047, essv6876376, essv6934590 | Samples | SSM083, SSM027, SSM046, SSM097, SSM093, SSM042, SSM002, SSM021, SSM089, SSM017, SSM032, SSM031, SSM001, SSM014, SSM033, SSM037, SSM095 | Known Genes | EXOC2 | 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) | esv2731363
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 17 | Observed Complex | 0 | Frequency | n/a |
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