How to handle Allele normalization for Range Locations
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2.0-alpha
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Stale-exempt
- Dominant language
- Python
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Description
One major theme raised in #234 is the question of "how do we handle Allele normalization when the Allele Location is specified by Ranges"? To me, these have always seemed to be a shorthand for "I did a targeted region assay and want to craft general statements about copy number in those regions and the potential broader impact they have". I know we allow people to create Alleles with Range-based Locations anyway, but... why? The PR supports those cases and raises interesting questions, e.g. what do we do with definite range intervals?
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