Variant DetailsVariant: esv2738040| Internal ID | 10321676 | | Landmark | | | Location Information | | | Cytoband | 10q21.3 | | Allele length | | Assembly | Allele length | | hg38 | 437 | | hg19 | 437 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv6672682, essv6705947, essv6684833, essv6850714, essv6891007, essv6755311, essv6702931, essv6685332, essv6912299, essv6812004, essv6736131 | | Samples | SSM097, SSM058, SSM031, SSM001, SSM086, SSM040, SSM007, SSM015, SSM005, SSM076, SSM034 | | Known Genes | SLC25A16 | | 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) | esv2738040
| | Frequency | | Sample Size | 96 | | Observed Gain | 0 | | Observed Loss | 11 | | Observed Complex | 0 | | Frequency | n/a |
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