Product Details
- Assay Reference Genome
Location
Chr.11:19375107 on build GRCh38
- Cytoband
- 11p15.1
- Species
- Homo sapiens
- Variation Type
- Copy Number
Additional Information
For this assay, SNP(s) [rs78453751] 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.
Target Gene Details
- Entrez Gene ID
- 89797
- Gene Symbol
- NAV2
- Gene Name
- neuron navigator 2
- Gene Aliases
- HELAD1, POMFIL2, RAINB1, STEERIN2, UNC53H2
- Location
- Chr.11:19345200-20121601 on build GRCh38
- Assay Gene Location
- Within Intron 2
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