Hi,
I am currently using the genome variants tracks on the genome browser and am
wondering the following:
If no variant is displayed for a given individual (e.g., YRI NA18507) at a
particular SNP does this mean that the individual has the same allele as the
human reference individual? Alternatively, does it mean there is no data
available for that individual due to some technical difficulty?
Thank you kindly,
Terence
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