Assay Details
Target Gene Details
Entrez Gene ID: | 100131626 |
Gene Name: | uncharacterized LOC100131626 |
Gene Aliases: |
- |
Location: |
Chr.11:118381220-118418815 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LOC100131626 | NR_046369.1 | |||
NR_046370.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2658105 | Chr.11:118410941 - 118412223 on Build GRCh38 | Deletion | LOC100131626 |
esv24734 | Chr.11:118411322 - 118411861 on Build GRCh38 | Loss | LOC100131626 |
esv3627869 | Chr.11:118410960 - 118412452 on Build GRCh38 | Loss | LOC100131626 |
More Information
Additional Information:
For this assay, SNP(s) [rs111993696] 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 Intronic Non-exonic DGV Variation |