Allele parent of origin - Added a new annotation on CNV-loss (deletions) showing the remaining allele parent of origin. This new annotation is displayed in the variant full details, on the variant assessment tab under the family zygosity table.
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Multi select variants - Allows to select multi variants and apply common actions on them at once. You can select a variant by marking the check-box to the left of the tile and applying the action from the suggested actions that will appear on the top part of the screen.
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Family merged filters - Added support to allow creation of merged filters in family cases. To read more about “merged filter” please go to the relevant article in Franklin’s Help center.
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Variant navigation - Now you can navigate to the next/previous variant on your list from the variant pop up. Just click on the arrows to the right/left of the variant pop up or use the keyboard shortcut “ctrl + <” for previous and “ctrl + >” for next variant
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Edit CNV breakpoints in Whole Genome and CMA workflows - Added support for selecting the breakpoints on the confidence graph.
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Batch name support in sample sheet - Added support in an additional field in the sample sheet that will allow marking samples as part of a batch

HPO number support - HPO numbers can be used when creating a case - both when using a sample sheet or when adding phenotypes directly in Franklni’s UI.

Improvements to the TSO 500 CNV calling model