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two variants nearly detected in NGS, a challenge!

Hi all

how can we interpret this?

two variants nearly detected in NGS (20 bps distance), in the reads which covers both of them we have: 20 % of reads have both variants 40 % of reads have only first variant 40 % of reads have only second variant

do you know what exactly happened which have made this result?

sequencing ngs wes wgs

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