Assay Details
Target Gene Details
Entrez Gene ID: | 55289 |
Gene Name: | acyl-CoA oxidase-like |
Gene Aliases: |
- |
Location: |
Chr.2:110732539-111118571 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 1 - Intron 1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv730e214 | Chr.2:110395308 - 110848620 on Build GRCh38 | Gain | LIMS4 LOC100288570 RGPD6 LOC105373553 BUB1 ACOXL SNORD132 |
nsv521956 | Chr.2:110634682 - 112341235 on Build GRCh38 | Loss | FBLN7 MIR4435-2 ZC3H8 LOC400997 BCL2L11 BUB1 ACOXL SNORD132 ZC3H6 PAFAH1B1P2 TMEM87B MIR4771-2 ANAPC1 MIR4435-2HG MERTK |
esv3591965 | Chr.2:110642083 - 110829253 on Build GRCh38 | Gain | BUB1 ACOXL SNORD132 |
dgv4047n100 | Chr.2:110308696 - 112358403 on Build GRCh38 | Loss | FBLN7 LOC105375809 MIR4435-2 LOC100288570 ZC3H8 LOC105373553 LOC400997 BCL2L11 BUB1 ACOXL SNORD132 ZC3H6 LIMS4 RGPD6 PAFAH1B1P2 TMEM87B MIR4771-2 ANAPC1 MIR4435-2HG LINC01106 MERTK |
More Information
Additional Information:
For this assay, SNP(s) [rs79918262] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic Non-exonic DGV Variation |